Multi-level specific targeting of cancer cells

ABSTRACT

A compound comprising, in combination: a cell surface binding ligand or internalizing factor, such as an IL-13Rα2 binding ligand; at least one effector molecule (e.g., one, two, three or more effector molecules); optionally but preferably, a cytosol localization element covalently coupled between said binding ligand and said at least one effector molecule; and a subcellular compartment localization signal element covalently coupled between said binding ligand and said at least one effector molecule (and preferably with said cytosol localization element between said binding ligand and said subcellular compartment localization signal element). Methods of using such compounds and formulations containing the same are also described.

RELATED APPLICATIONS

This application is a continuation of and claims priority to U.S. patentapplication Ser. No. 13/086,698, filed Apr. 14, 2011, now allowed, whichclaims the benefit of U.S. Provisional Patent Application Ser. No.61/324,952, filed Apr. 16, 2010, the disclosure of each of which isincorporated by reference herein in its entirety.

GOVERNMENT FUNDING

This invention was made with United States government support undergrant number RO1 CA 74145 from the National Institutes of Health. TheUnited States government has certain rights to this invention.

FIELD OF THE INVENTION

The present invention concerns methods and constructs for deliveringcompounds of interest to cells, particularly cells that express IL-13receptors.

BACKGROUND OF THE INVENTION

Molecular targeting of cancer cells is achieved (a) specifically throughthe use of ligands/antibodies against tumor-associated or tumor-specificreceptors, and (b) non-specifically using plasma membrane permeableagents targeting activated/over-expressed intracellular elements, suchas the oncogenes. In the field of non-viral gene therapy of cancer thatemploys recombinant proteins, the inventors have pioneered the use ofproteinaceous vectors for the targeted intracellular transport ofproteins/non-proteinaceous compounds (1-3). Some bacterial toxins, suchas Pseudomonas exotoxin A (PE) or Diphtheria toxin (DT), possess anability to exit the endocytic compartment after being internalized inthe process of receptor-mediated internalization and beingproteolytically activated by a calcium-dependent serine endoprotease,furin (4-7). This “get cleaved and exit endocytic compartment” abilityis possible due to the presence of a specialized domain of PE, domain II(abbreviated here D2) (8; 9).

Previously, the inventors have exploited PE translocation ability totraffic other, non-PE, or repeated PE peptide sequences into the cellcytosol (1). This was achieved by incorporating non-PE peptides or anadditional catalytic domain III of PE within dispensable domain Ib. Thisdomain is downstream of both furin cleavage site and a cleavage-createdN-terminal sequence important for initiation/conduct of the C-terminalportion of the toxin (portion of domain 2 and domain 3) endocyticvesicles exit. The inventors demonstrated for the first time that inthis manner, PE can serve as a vector for intra-cytosolic delivery ofvarious proteins (1).

Most anti-cancer therapeutics have defined targets such as oncogenes,enzymes or DNA, all of which are localized to distinct intra-cellularcompartments like nucleus, mitochondria or cytosol. GBM is a high-gradeastrocytoma representing the most common form of primary brain tumors.The successful treatment of patients with GBM is still a major challengeand the median survival rate is 14.5 months after diagnosis (12).Several factors specific to GBM have been uncovered in recent years(13-16). For example, a tri-molecular signature of GBM has beendocumented that includes IL-13Rα2, EphA2 receptor and a fos-relatedantigen 1 (Fra-1) (17). All three factors belonging to the signature aresuitable for therapeutic targeting of GBM (18). IL-13Rα2 is expressedin >75% of GBM tumor specimens (19; 20) and is characterized as acancer/testes like antigen (21). IL-13Rα2 is believed to act as a decoyreceptor (22). However, it has been shown that IL-13 ligand binds toIL13Rα2 receptor and is internalized through receptor mediatedendocytosis (23; 24). Thus, drugs attached to the IL-13 ligand can beinternalized and delivered specifically inside the glioma cells.

SUMMARY OF THE INVENTION

A first aspect of the invention is a compound comprising, incombination: a cell surface binding ligand or internalizing factor, suchas an IL-13Rα2 binding ligand; at least one effector molecule (e.g.,one, two, three or more effector molecules); optionally but preferably,a cytosol localization element covalently coupled between said bindingligand and said at least one effector molecule; and a subcellularcompartment localization signal element covalently coupled between saidbinding ligand and said at least one effector molecule (and preferablywith said cytosol localization element between said binding ligand andsaid subcellular compartment localization signal element).

In some embodiments, the compound has the formula, from N terminus to Cterminus, selected from the group consisting of: A-B-C-D-E; E-D-C-B-A;A-B-D-C-E; and E-C-D-B-A, wherein: A is an internalizing factor orbinding element such as an IL-13Rα2 binding ligand; B is the cytosollocalization element; C is the subcellular compartment localizationsignal element; D is present or absent and when present a first effectormolecule; and E is present or absent and when present is a secondeffector molecule. As will be appreciated, additional effector molecules(e.g., three or more effector molecules) can be included if so desired.

In some embodiments, the compound is a fusion protein or covalentconjugate.

In some embodiments, each of A, B, and C, and optionally D and E, is apeptide.

In some embodiments, the cytosol localization element is a Pseudomonasor diphtheria toxin translocation domain, such as a Pseudomonas exotoxinA D2 segment.

In some embodiments, the subcellular compartment localization signalelement is a nuclear localization element or a lysosomal localizationelement, such as an SV40 T antigen nuclear localization signal.

In some embodiments, wherein said IL-13Rα2 binding ligand is IL-13, amutant of IL-13, or an IL-13Rα2 binding fragment thereof.

A further aspect of the invention is a nucleic acid that encodes acompound as described above, along with host cells that contain andexpress the same.

A further aspect of the invention is a method of treating and/ordetecting cancer in a subject in need thereof, comprising administeringsaid subject a compound as described herein in a treatment and/ordetection effective amount. The cancer may be, for example, breastcancer, bladder cancer, pancreatic cancer, colorectal cancer, head andneck cancer, thyroid cancer, prostate cancer, and gliomas such asglioblastoma multiforme.

A further aspect of the invention is a method of detecting IL-13Rα2expressing cells, comprising administering a compound as describedherein to a cell or group of cells in vitro or in vivo, and detecting adetectable group coupled to said compound.

A further aspect of the invention is a method of delivering at least oneeffector molecule (e.g., a detectable group or a therapeutic group) to asubcellular compartment of a cell of interest, comprising: contacting acompound as described herein including at least one effector molecule(e.g., as either D or E) to a cell of interest (e.g., a eukaryotic cell,in vitro or in vivo) under conditions in which said compound isinternalized therein and said effector molecule is delivered to saidsubcellular compartment (e.g., the nucleus). In some embodiments, thecompound further comprises an additional effector molecule (e.g., aseither D or E). In some embodiments, the additional effector molecule isdelivered to the cytosol of the cell of interest (e.g., wherein saidcompound is of the formula A-B-D-C-E or E-C-D-B-A). The method is usefulfor research purposes (e.g., labeling subcellular compartments), and forthe methods of diagnosis and treatment described herein.

A further aspect of the invention is the use of a compound as describedherein for carrying out a method as described herein, and/or for thepreparation of a medicament as described herein.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention is explained in greater detail below. Thisdescription is not intended to be a detailed catalog of all thedifferent ways in which the invention may be implemented, or all thefeatures that may be added to the instant invention. For example,features illustrated with respect to one embodiment may be incorporatedinto other embodiments, and features illustrated with respect to aparticular embodiment may be deleted from that embodiment. In addition,numerous variations and additions to the various embodiments suggestedherein will be apparent to those skilled in the art in light of theinstant disclosure which do not depart from the instant invention.Hence, the following specification is intended to illustrate someparticular embodiments of the invention, and not to exhaustively specifyall permutations, combinations and variations thereof.

The disclosures of all United States patents cited herein are to beincorporated herein by reference in their entirety.

A. DEFINITIONS

“Capping group” as used herein includes, but is not limited to, acetyl,benzoyl, formyl, trifluoroacetyl, benzyloxycarbonyl,tert-butyloxycarbonyl, biphenylylisopropyloxycarbonyl, triphenylmethyl,o-nitrobenzenesulfenyl, and diphenylphosphinyl. The capping groups mayconsist of such groups as R¹⁰CO—, R¹⁰—O—CO—, R¹⁰—PO—, R¹⁰—SO₂— andarylalkyl-; where R¹⁰ is selected from the group consisting of H, alkyl,alkenyl, alkynyl, aryl, and arylalkyl.

“Alkyl,” as used herein, refers to a straight or branched chainhydrocarbon containing from 1 to 10 carbon atoms. Representativeexamples of alkyl include, but are not limited to, methyl, ethyl,n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl,n-pentyl, isopentyl, neopentyl, n-hexyl, 3-methylhexyl,2,2-dimethylpentyl, 2,3-dimethylpentyl, n-heptyl, n-octyl, n-nonyl,n-decyl, and the like. “Loweralkyl” as used herein, is a subset of alkyland refers to a straight or branched chain hydrocarbon group containingfrom 1 to 4 carbon atoms. Representative examples of lower alkylinclude, but are not limited to, methyl, ethyl, n-propyl, iso-propyl,n-butyl, iso-butyl, tert-butyl, and the like.

“Alkenyl,” as used herein, refers to a straight or branched chainhydrocarbon containing from 2 to 10 carbons and containing at least onecarbon-carbon double bond formed by the removal of two hydrogens.Representative examples of “alkenyl” include, but are not limited to,ethenyl, 2-propenyl, 2-methyl-2-propenyl, 3-butenyl, 4-pentenyl,5-hexenyl, 2-heptenyl, 2-methyl-1-heptenyl, 3-decenyl and the like.“Lower alkenyl” as used herein, is a subset of alkenyl and refers to astraight or branched chain hydrocarbon group containing from 2 to 4carbon atoms.

“Alkynyl,” as used herein, refers to a straight or branched chainhydrocarbon group containing from 2 to 10 carbon atoms and containing atleast one carbon-carbon triple bond. Representative examples of alkynylinclude, but are not limited, to acetylenyl, 1-propynyl, 2-propynyl,3-butynyl, 2-pentynyl, 1-butynyl and the like. “Lower alkynyl” as usedherein, is a subset of alkyl and refers to a straight or branched chainhydrocarbon group containing from 2 to 4 carbon atoms.

The alkyl, alkenyl, and alkynyl groups of the invention can besubstituted or unsubstituted and are either unless otherwise specified.When substituted the alkyl, alkenyl or alkynyl groups of the inventioncan be substituted with 1, 2, 3, 4, or 5 or more substituentsindependently selected from alkenyl, alkenyloxy, alkoxy, alkoxyalkoxy,alkoxycarbonyl, alkyl, alkylcarbonyl, alkylcarbonyloxy, alkylsulfinyl,alkylsulfonyl, alkylthio, alkynyl, aryl, azido, arylalkoxy, arylalkyl,aryloxy, carboxy, cyano, formyl, halogen, haloalkyl, haloalkoxy,hydroxy, hydroxyalkyl, mercapto, nitro, sulfamyl, sulfo, sulfonate,

“Aryl” as used herein, refers to a monocyclic carbocyclic ring system ora bicyclic carbocyclic fused ring system having one or more aromaticrings. Representative examples of aryl include, azulenyl, indanyl,indenyl, naphthyl, phenyl, tetrahydronaphthyl, and the like.

The aryl groups of this invention can be substituted with 1, 2, 3, 4, or5 or more substituents independently selected from alkenyl, alkenyloxy,alkoxy, alkoxyalkoxy, alkoxycarbonyl, alkyl, alkylcarbonyl,alkylcarbonyloxy, alkylsulfinyl, alkylsulfonyl, alkylthio, alkynyl,aryl, azido, arylalkoxy, arylalkyl, aryloxy, carboxy, cyano, formyl,halogen, haloalkyl, haloalkoxy, hydroxy, hydroxyalkyl, mercapto, nitro,sulfamyl, sulfo, sulfonate,

“Arylalkyl,” as used herein, refers to an aryl group, as defined herein,appended to the parent molecular moiety through an alkenyl group, asdefined herein. Representative examples of arylalkenyl include, but arenot limited to, 2-phenylethenyl, 3-phenylpropen-2-yl,2-naphth-2-ylethenyl, and the like, which may be substituted orunsubstituted as noted above.

“IL13” or “IL-13” as used herein refers to interleukin-13, which is apleiotropic cytokine. IL-13 has approximately 30% sequence identity withIL4 and exhibits IL4-like activities on monocytes/macrophages and humanB cells (Minty et al. (1993) Nature 362:248; McKenzie et al. (1987)Proc. Natl. Acad. Sci. USA 90:3735). In particular, IL-13 appears to bea potent regulator of inflammatory and immune responses. IL-13 canup-regulate the monocyte/macrophage expression of CD23 and MHC class Iand class II antigens, down-regulate the expression of Fc.gamma, andinhibit antibody-dependent cytotoxicity. IL-13 can also inhibit nitricoxide production as well as the expression of pro-inflammatory cytokines(e.g., IL-1, IL-6, IL-8, IL-10 and IL-12) and chemokines (MIP-1, MCP),but enhance the production of IL-1.

“Recombinant” nucleic acid as used herein refers to a nucleic acidproduced by combining two or more nucleic acid sequences from differentsources, e.g., by use of molecular biology techniques, to form a newnucleic acid, e.g., a “heterologous” nucleic acid. The recombinantnucleic acid may be provided in the form of a “vector” or “deliveryvector” in order to transform or transfect cells to contain the newnucleic acid. As used herein, a “vector” or “delivery vector” can be aviral or non-viral vector that is used to deliver a nucleic acid to acell, tissue or subject.

A “recombinant” protein is a protein produced by a recombinant nucleicacid. The nucleic acid may or may not be inserted into the genome of ahost cell. The nucleic acid may exist, e.g., in plasmid form in a hostcell. Alternatively, the recombinant protein may be produced by in vitrotranslation of the recombinant nucleic acid.

An “isolated” protein or polypeptide means a protein or polypeptide thatis separated or substantially free from at least some of the othercomponents of the naturally occurring organism or virus, for example,the cell or viral structural components or other proteins or nucleicacids commonly found associated with the protein. As used herein, the“isolated” protein or polypeptide is at least about 25%, 30%, 40%, 50%,60%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99% or more pure (w/w).

“Subjects” as used herein are generally human subjects and includes, butis not limited to, cancer patients. The subjects may be male or femaleand may be of any race or ethnicity, including, but not limited to,Caucasian, African-American, African, Asian, Hispanic, Indian, etc. Thesubjects may be of any age, including newborn, neonate, infant, child,adolescent, adult, and geriatric. Subjects may also include animalsubjects, particularly mammalian subjects such as canines, felines,bovines, caprines, equines, ovines, porcines, rodents (e.g. rats andmice), lagomorphs, primates (including non-human primates), etc.,screened for veterinary medicine or pharmaceutical drug developmentpurposes.

“Cancer” or “cancers” that can be detected and/or treated by thecompounds, compositions and methods described herein include, but arenot limited to, breast cancer, bladder cancer, pancreatic cancer,colorectal cancer, head and neck cancer, thyroid cancer, prostatecancer, and brain cancer such as gliomas (e.g., GBM), etc.

“Effector molecule” as used herein includes therapeutic agents,detectable groups, targeting ligands, and delivery vehicles (e.g.,antibodies, lipids, liposomes). See, e.g., U.S. Pat. No. 6,630,576.

“Therapeutic agent” as used herein may be any therapeutic agentincluding, but not limited to, genetic materials or agents,radionuclides, chemotherapeutic agents, and cytotoxic agents (See, e.g.,U.S. Pat. No. 6,949,245 to Sliwkowski), and amphipathic antimicrobialpeptides. Other exemplary therapeutic agents include, but are notlimited to, radiopharmaceuticals, including, but not limited to augerelectrons, chemotherapeutics, and photosensitizers.

“Radionuclide” as described herein includes, but is not limited to,²²⁷Ac, ²¹¹At, ¹³¹Ba, ⁷⁷Br, ¹⁰⁹Cd, ⁵¹Cr, ⁶⁷Cu, ¹⁶⁵Dy, ¹⁵⁵Eu, ¹⁵³Gd,¹⁹⁸Au, ¹⁶⁶Ho, ^(113m)In, ^(115m)In, ¹²³I, ¹²⁵I, ¹³¹I, ¹⁸⁹Ir, ¹⁹¹Ir,¹⁹²Ir, ¹⁹⁴Ir, ⁵²Fe, ⁵⁵Fe, ⁵⁹Fe, ¹⁷⁷Lu, ¹⁰⁹Pd, ³²P, ²²⁶Ra, ¹⁸⁶Re, ¹⁸⁸Re,¹⁵³Sm, ⁴⁶Sc, ⁴⁷Sc, ⁷²Se, ⁷⁵Se, ¹⁰⁵Ag, ⁸⁹Sr, ³⁵S, ¹⁷⁷Ta, ¹¹⁷mSn, ¹²¹Sn,¹⁶⁶Yb, ¹⁶⁹Yb, ⁹⁰Y, ²¹²Bi, ¹¹⁹Sb, ¹⁹⁷Hg, ⁹⁷Ru, ¹⁰⁰Pd, ^(101m)Rh, and²¹²Pb.

“Chemotherapeutic agent” as used herein includes, but is not limited to,methotrexate, daunomycin, mitomycin C, cisplatin, vincristine,epirubicin, fluorouracil, verapamil, cyclophosphamide, cytosinearabinoside, aminopterin, bleomycin, mitomycin C, democolcine,etoposide, mithramycin, chlorambucil, melphalan, daunorubicin,doxorubicin, tamosifen, paclitaxel, vincristin, vinblastine,camptothecin, actinomycin D, and cytarabine. Other examples are found inU.S. Patent Application Publication 2006/0121539 (Debinski et al.),which is incorporated by reference herein in its entirety.

“Cytotoxic agent” or “toxic agent” as used herein includes, but is notlimited to, maytansinoids and maytansinoid analogs, taxoids, CC-1065 andCC-1065 analogs, dolastatin and dolastatin analogs, ricin (or moreparticularly the ricin A chain), aclacinomycin, Diphtheria toxin,Monensin, Verrucarin A, Abrin, Tricothecenes, and Pseudomonas exotoxinA, taxol, cytochalasin B, gramicidin D, ethidium bromide, emetine,mitomycin, etoposide, tenoposide, anti-mitotic agents, such as the vincaalkaloids (e.g., vincristine and vinblastine), colchicin,anthracyclines, such as doxorubicin and daunorubicin, dihydroxyanthracin dione, mitoxantrone, mithramycin, actinomycin D,1-dehydrotestosterone, glucocorticoids, procaine, tetracaine, lidocaine,propranolol, and puromycin and analogs or homologs thereof,antimetabolites (e.g., methotrexate, 6-mercaptopurine, 6-thioguanine,cytarabine, and 5-fluorouracil decarbazine), alkylating agents (e.g.,mechlorethamine, thioepa chlorambucil, melphalan, carmustine (BSNU),lomustine (CCNU), cyclothosphamide, busulfan, dibromomannitol,streptozotocin, mitomycin C, and cis-dichlorodiamine platinum (II)(DDP)), and antibiotics, including, but not limited to, dactinomycin(formerly actinomycin), bleomycin, mithramycin, calicheamicin, andanthramycin (AMC)).

In some embodiments, cytotoxic agents include toxins such as Pseudomonasexotoxin, ricin, abrin, ribonuclease (RNase), DNase I, Staphylococcalenterotoxin-A, pokeweed antiviral protein, gelonin, diphtheria toxin,etc. See, e.g., U.S. Pat. No. 7,517,964. In some embodiments,Pseudomonas exotoxin or a Diphtheria toxin are preferred. See U.S. Pat.No. 5,328,984 to Pastan et al. and U.S. Pat. No. 6,296,843 to Debinski,which are each incorporated by reference herein in its entirety.Pseudomonas exotoxins can include, but are not limited to, Pseudomonasexotoxin A (PE). The Pseudomonas exotoxin can be modified such that itsubstantially lacks domain Ia, and in some embodiments Pseudomonasexotoxins include PE38QQR and PE4E. Diphtheria toxins can include DT390,a diphtheria toxin in which the native binding domain is eliminated. Itwill be appreciated that in various embodiments, the therapeutic agentscan be attached to, e.g., the amino terminus or the carboxyl terminus.

“Amphipathic antimicrobial peptide” as used herein includes amphipathicpeptides that induce apoptosis of cancer cells, presumably through theirability to depoarize mitochondrial membranes. K. Rege et al., CancerRes. 67, 6368 (Jul. 1, 2007). Such peptides are, in general, from 10, 12or 13 to 20, 30 or 40 amino acids in length, or more, and typically havean amphipathic alpha-helical structure. Examples include, but are notlimited to, (KLAKLAK)₂ (SEQ ID NO: 60); (KLAKKLA)₂ (SEQ ID NO: 61)(KAAKKAA)₂ (SEQ ID NO: 62) and (KLGKKLG)₂ (SEQ ID NO: 63) See, e.g.,Ruoslahti et al., US Patent Application 20010046498 (Nov. 29, 2001).

“Detectable group” or “label” as used herein includes, but is notlimited to, radiolabels (e.g., ³⁵S, ¹²⁵I, ³²P, ³H, ¹⁴C, ¹³¹I), enzymelabels (e.g., horseradish peroxidase, alkaline phosphatase), gold beads,chemiluminescence labels, ligands (e.g., biotin, digoxin) and/orfluorescence labels (e.g., rhodamine, phycoerythrin, fluorescein,fluorescent proteins), a fluorescent protein including, but not limitedto, a green fluorescent protein or one of its many modified forms, anucleic acid segment in accordance with known techniques, and energyabsorbing and energy emitting agents. Thus “label” or “detectable group”as used herein may be any suitable label or detectable group detectableby spectroscopic, photochemical, biochemical, immunochemical,electrical, optical or chemical means including but not limited tobiotin, fluorophores, antigens, porphyrins, and radioactive isotopes.Labels useful in the present invention include biotin for staining withlabeled avidin or streptavidin conjugate, magnetic beads (e.g.,Dynabeads™), fluorescent dyes (e.g., fluorescein,fluorescein-isothiocyanate [FITC], Texas red, rhodamine, greenfluorescent protein, enhanced green fluorescent protein, lissamine,phycoerythrin, Cy2, Cy3, Cy3.5, Cy5, Cy5.5, Cy7, Fluor X [Amersham],SyBR Green I & II [Molecular Probes], and the like), radiolabels (e.g.,³H, ³⁵S, ¹⁴C, or ³²P), enzymes (e.g., hydrolases, particularlyphosphatases such as alkaline phosphatase, esterases and glycosidases,or oxidoreductases, particularly peroxidases such as horseradishperoxidase, and the like), substrates, cofactors, inhibitors,chemiluminescent groups, chromogenic agents, and calorimetric labelssuch as colloidal gold or colored glass or plastic (e.g., polystyrene,polypropylene, latex, etc.) beads.

“Treat,” “treating” or “treatment” as used herein refers to any type oftreatment that imparts a benefit to a patient afflicted with a disease,including improvement in the condition of the patient (e.g., in one ormore symptoms), delay in the progression of the disease, etc.

“Pharmaceutically acceptable” as used herein means that the compound orcomposition is suitable for administration to a subject to achieve thetreatments described herein, without unduly deleterious side effects inlight of the severity of the disease and necessity of the treatment.

“Concurrently administering” or “concurrently administer” as used hereinmeans that the two or more compounds or compositions are administeredclosely enough in time to produce a combined effect (that is,concurrently may be simultaneously, or it may be two or more eventsoccurring within a short time period before or after each other, e.g.,sequentially). Simultaneous concurrent administration may be carried outby mixing the compounds prior to administration, or by administering thecompounds at the same point in time but at different anatomic sitesand/or by using different routes of administration.

“Internalizing factor” as used herein may be any compound or constructthat binds to a cell surface protein which is then taken up into thecell by binding. Numerous such internalizing factors are known,including but not limited to those described in D. Curiel et al., U.S.Pat. Nos. 6,274,322 and 6,022,735, the disclosures of which areincorporated herein by reference.

The definitions and techniques described herein also apply to the IL-13targeting peptides, toxin proteins, and other compounds and compositionsmentioned hereinabove and hereinbelow.

B. TARGETING PEPTIDES THAT BIND TO THE IL-13 BINDING SITE

In some embodiments of the invention, the internalizing factor,targeting protein, peptide or agent is IL-13 or a fragment thereof thatspecifically binds the IL-13 receptor. The terms “peptide,”“polypeptide,” and “protein” are used interchangeably and refer to anypolymer of amino acids (dipeptide or greater) linked through peptidebonds. Recombinant IL-13 is commercially available from a number ofsources (e.g., R&D Systems, Minneapolis, Minn., and SanofiBio-Industries, Inc., Tervose, Pa.). Alternatively, a gene or cDNAencoding IL-13 may be cloned into a plasmid or other expression vectorand expressed in any of a number of expression systems according tomethods well known to those of skill in the art. Methods of cloning andexpressing IL-13 and the nucleic acid sequence for IL-13 are well known(see, for example, Minty et al. (1993) supra and McKenzie (1987) supra).In addition, the expression of IL-13 as a component of a chimericmolecule is detailed below. Also contemplated is the use of specificIL-13 mutants or a fragment thereof as described in U.S. Pat. No.6,884,603 (Debinski et al.). An exemplary IL-13 mutant is IL-13.E13K,which has an amino acid residue at position 13 substituted for lysine.

One of skill in the art will appreciate that analogues or fragments ofIL-13 or IL-13 mutants will also specifically bind to the IL-13receptor. For example, conservative substitutions of residues (e.g., aserine for an alanine or an aspartic acid for a glutamic acid)comprising native IL-13 will provide IL-13 analogues that alsospecifically bind to the IL-13 receptor. Thus, the terms “IL-13” or“IL-13 mutant” when used in reference to a targeting molecule, alsoincludes fragments, analogues or peptide mimetics of IL-13 or IL-13mutants that also specifically bind to the IL-13 receptor. Furtherdiscussion of IL-13 as contemplated by the present invention can befound in U.S. Pat. Nos. 5,328,984 (Pastan et al.), 5,614,191 (Puri etal.), 5,919,456 (Puri et al.), 6,296,843 (Debinski), 6,428,788 (Debinskiet al.), 6,518,061 (Puri et al.), 6,576,232 (Debinski et al.), 6,630,576(Debinski), and 6,884,603 (Debinski et al.).

In some embodiments of the present invention the targeting proteinspecifically binds to the IL-13Rα2 receptor. As described above thetargeting protein that specifically binds to the IL-13Rα2 receptor maybe IL-13, a mutant of IL-13, or a fragment thereof.

The targeting peptides of the present invention can be coupled to orconjugated to effector molecules, cytosol localization elements, orsubcellular compartment localization signal elements by any suitabletechnique, including those described further in “Conjugates” below. Thedescribed conjugates can be used for therapeutic and/or diagnosticpurposes.

C. TARGETING PEPTIDES THAT DO NOT BIND TO THE IL-13 BINDING SITE

In some embodiments, the internalizing factor or targeting peptides ofthe present invention are not IL-13 or IL-13 mutants and/or fragments,but instead are peptides that do not bind to the IL-13 binding site, butinstead bind to a different binding site on the IL-13 receptor.

The single letter code for amino acids as used herein is: A (Ala), C(Cys), D (Asp), E (Glu), F (Phe), G (Gly), H (His), I (Ile), K (Lys), L(Leu), M (Met), N (Asn), P (Pro), Q (Gln), R (Arg), S (Ser), T (Thr), V(Val), W (Trp), and Y (Tyr)).

In some embodiments, targeting peptides of the present invention canhave the general formula, from amino terminus to carboxy terminus, oralternatively from carboxy terminus to aminuo terminus, of FORMULA I:

X—R¹—R²—R³—R⁴—R⁵—R⁵—R⁶—R⁷—Y  (I)

wherein:

R¹ is G or S;

R² is a negatively charged amino acid (for example E or D);

R³ is a large hydrophobic amino acid (for example M, W, Y, or, I);

R⁴ is a small amino acid (for example G, S or A);

R⁵ is a large or aromatic amino acid (for example W, F, H or Y);

R⁶ is a preferably hydrophobic or neutral amino acid (for example V, P,T or N);

R⁷ is a positively charged amino acid (for example R, K or H); and

X and Y are as given below.

In other embodiments, targeting peptides of the present invention canhave the general formula, from amino terminus to carboxy terminus, oralternatively from carboxy terminus to aminuo terminus, of FORMULA II:

X—R¹—R²—R³—R⁴—R⁵—R⁵—R⁶—R⁷—Y  (II)

wherein:

R¹ is a hydrophobic amino acid (for example L, A, I, V, or M);

R² is a preferably hydrophobic or neutral amino acid (for example P, V,T or N);

R³ is a charged or uncharged polar amino acid (for example Q, N, D, E orH)

R⁴ is a hydrophobic amino acid (for example L, A, I, V, or M);

R⁵ is large or aromatic amino acid (for example W, F, H or Y);

R⁶ is a hydrophobic amino acid (for example L, A, I, V, or M);

R⁷ is large or aromatic amino acid (for example F, W, H or Y); and

X and Y are as described below.

In still other embodiments, targeting peptides of the present inventioncan have the general formula, from amino terminus to carboxy terminus,or alternatively from carboxy terminus to aminuo terminus, of FORMULAIII:

X—R¹—R²—R³—R⁴—R⁵—R⁵—R⁶—R⁷—Y  (III)

wherein:

R¹ is S or G;

R² is a preferably hydrophobic or neutral amino acid (for example, P, V,T or N);

R³ is large or aromatic amino acid (for example F, W, H or Y);

R⁴ is a hydrophobic amino acid (for example, L, A, I, V, or M);

R⁵ is large or aromatic amino acid (for example H, W, F, or Y);

R⁶ is a hydrophobic amino acid (for example L, A, I, V, or M);

R⁷ is a hydrophobic amino acid (for example L, A, I, V, or M); and

X and Y are as described below.

In Formulas I-III, X and Y can each independently be present or absentand when present can each independently be a capping group, a linkinggroup (or “linker”, including non-amino acid linking groups, see, e.g.,U.S. Pat. Nos. 7,468,418; 7402,652; and 7,351,797), an amino acid (e.g.C, S or G) optionally terminated by a capping group or linking group, ora peptide consisting of from 2 to 6 or 10 additional amino acidsoptionally terminated by a capping group or linking group.

The amino acids of peptides of the invention may be in D form, L form,or a combination thereof.

Specific examples of targeting peptides of FORMULAS I-III include, butare not limited to those set forth in Tables 1-3 and Tables 4-6 below.These peptides may or may not have linking groups bonded to the carboxyterminus. Linking groups as used herein are described in more detailbelow.

Active compounds of the present invention can be produced by anysuitable means, including by synthetic organic chemical techniques or byrecombinant techniques in which a nucleic acid that encodes the activecompound is produced and introduced into a host cell (typically in theform of an expression vector) so that the encoded active compound(peptide, fusion peptide, etc.) is expressed therein. Expression vectorscan be designed for expression of proteins or polypeptides inprokaryotic or eukaryotic cells. For example, polypeptides can beexpressed in bacterial cells such as E. coli, insect cells (e.g., in thebaculovirus expression system), yeast cells or mammalian cells. Suitablehost cells are discussed further in Goeddel, Gene Expression Technology:Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990).Examples of vectors for expression in yeast S. cerevisiae includepYepSec1 (Baldari et al, (1987) EMBO J. 6:229-234), pMFa (Kurjan andHerskowitz (1982) Cell 30:933-943), pJRY88 (Schultz et al. (1987) Gene54:113-123), and pYES2 (Invitrogen Corporation, San Diego, Calif.).Baculovirus vectors available for expression of nucleic acids to produceproteins in cultured insect cells (e.g., Sf 9 cells) include the pAcseries (Smith et al. (1983) Mol. Cell. Biol. 3:2156-2165) and the pVLseries (Lucklow & Summers (1989) Virology 170:31-39).

Vectors can be introduced into prokaryotic or eukaryotic cells viaconventional transformation or transfection techniques. As used herein,the terms “transformation” and “transfection” refer to a variety ofart-recognized techniques for introducing foreign nucleic acids (e.g.,DNA) into a host cell, including calcium phosphate or calcium chlorideco-precipitation, DEAE-dextran-mediated transfection, lipofection,electroporation, microinjection, DNA-loaded liposomes, lipofectamine-DNAcomplexes, cell sonication, gene bombardment using high velocitymicroprojectiles, and viral-mediated transfection. Suitable methods fortransforming or transfecting host cells can be found in Sambrook et al.(Molecular Cloning: A Laboratory Manual, 2nd Edition, Cold Spring HarborLaboratory press (1989)), and other laboratory manuals.

TABLE 1 Peptides of Formula I CGEMGWVRC; (SEQ ID NO: 1) andACGEMGWVRCGGGS. (SEQ ID NO: 2)

TABLE 2 Peptides of Formula II CLPQLWLFC; (SEQ ID NO: 3) ACLPQLWLFCGGGS;(SEQ ID NO: 4)

TABLE 3 Peptides of Formula III CSPFLHLLC; (SEQ ID NO: 5) andACSPFLHLLCGGGS. (SEQ ID NO: 6)

TABLE 4 Additional Peptides of Formula I SEMGWVRC (SEQ ID NO: 7) GDMGWVR(SEQ ID NO: 8) SDWGWVR (SEQ ID NO: 9) GDYGWVR (SEQ ID NO: 10) SEIGWVRSEQ ID NO: 11) GEISWVR (SEQ ID NO: 12) GEMAWVR (SEQ ID NO: 13) GEMGFVR(SEQ ID NO: 14) GEMGHVR (SEQ ID NO: 15) GEMSYVR (SEQ ID NO: 16) GEMGWPR(SEQ ID NO: 17) GEMGWTR (SEQ ID NO: 18) GEMGWNK (SEQ ID NO: 19) GEMGWNH(SEQ ID NO: 20)

TABLE 5 Additional Peptides of Formula II APQLWLF (SEQ ID NO: 21)IPQLWLF (SEQ ID NO: 22) VPQLWLF (SEQ ID NO: 23) MPQLWLF (SEQ ID NO: 24)LVQLWLF (SEQ ID NO: 25) LTQLWLF (SEQ ID NO: 26) LNQLWLF (SEQ ID NO: 27)LPNLWLF (SEQ ID NO: 28) LPDLWLF (SEQ ID NO: 29) LPELWLF (SEQ ID NO: 30)LPHLWLF (SEQ ID NO: 31) LPQAFAW (SEQ ID NO: 32) LPQIFIH (SEQ ID NO: 33)LPQVHVY (SEQ ID NO: 34) LPQMYMY (SEQ ID NO: 35) MNHMYMY (SEQ ID NO: 36)VTEVHVH (SEQ ID NO: 37)

TABLE 6 Additional Peptides of Formula III GPFLHLL (SEQ ID NO: 38)SVFLHLL (SEQ ID NO: 39) STFLHLL (SEQ ID NO: 40) SNWLHLL (SEQ ID NO: 41)SPHLHLL (SEQ ID NO: 42) SPYLHLL (SEQ ID NO: 43) SPFAHLL (SEQ ID NO: 44)SPFIHLL (SEQ ID NO: 45) SPFVHLL (SEQ ID NO: 46) SPFMHLL (SEQ ID NO: 47)SPFLWLL (SEQ ID NO: 48) SPFLFAA (SEQ ID NO: 49) SPFLFII (SEQ ID NO: 50)SPFLHVV (SEQ ID NO: 51) SPFLYMM (SEQ ID NO: 52) GNYMYMM (SEQ ID NO: 53)GTHVFVI (SEQ ID NO: 54)

D. CONJUGATES

Targeting peptides as described herein may be coupled to or conjugatedto an effector molecule such as a diagnostic and/or therapeutic agent inaccordance with any of a variety of techniques, such as those employedin the production of immunoconjugates. See, e.g., U.S. Pat. No.6,949,245 to Sliwkowski.

In some embodiments, recombinant fusion chimera protein anti-cancercytotoxins are composed of a carrier/ligand and an effector (catalyst).Carrier/ligands can be proteinaceous compounds, such as growth factors,cytokines, and monoclonal antibodies, Among effectors, bacterial toxins,such as Pseudomonas exotoxin A and Diphtheria toxin, or plant toxins,such as ricin may be utilized in some embodiments. The fusion protein istargeted only to cells expressing a target receptor/adaptor for acarrier/ligand. These targets internalize in response to carrier/ligandbinding. Targets include, but are not limited to, protein receptors,antigens of various nature, adhesion molecules, gangliosides, etc. Forexample, EphA2 is over-expressed in a majority of patients with GBM andits ligand induces a receptor-mediated internalization once it binds thereceptor (Walker-Daniels et al. (2002) Mol. Cancer. Res. 1:79-87). Thelatter may be used for, e.g., recombinant bacterial toxin-containingcytotoxins to exert anti-tumor action (Debinski (2002) Molecular“Targeting of Brain Tumors with Cytotoxin,” In: Chimeric Toxins(Lorberboum-Galski & Lazarovici, eds., Harwood Academic Publishers) pp.222-246; Debinski (2002) Cancer Invest. 20:801-809; Debinski (2002)Cancer Invest. 20:801-809). Another non-limited example is the IL-13Rα2receptor whose ligand is internalized through receptor mediatedendocytosis.

Chemotherapeutic agents useful in the generation of such activecompounds include those described above. Conjugates of targeting peptideand one or more small molecule toxins, such as a calicheamicin, amaytansine (See U.S. Pat. No. 5,208,020), a trichothene, and CC 1065 arealso contemplated herein. In some embodiments, conjugates of targetingpeptide to Pseudomonas exotoxins are used (U.S. Pat. No. 5,328,984 toPastan et al.).

In some embodiments of the invention, the targeting peptide conjugatedto one or more maytansine molecules (e.g., about 1 to about 10maytansine molecules per targeting peptide molecule). Maytansine may,for example, be converted to May-SS-Me which may be reduced to May-SH3and reacted with modified targeting peptide (Chari et al. (1992) CancerRes. 52: 127-131) to generate an active compound.

Another conjugate of interest includes a targeting peptide conjugated toone or more calicheamicin molecules. The calicheamicin family ofantibiotics is capable of producing double-stranded DNA breaks atsub-picomolar concentrations. Structural analogues of calicheamicin thatmay be used include, but are not limited to, γ₁ ¹, α₂ ¹, α₃ ¹,N-acetyl-γ₁ ¹, PSAG and θ₁ ¹, (Hinman et al. (1993) Cancer Res.53:3336-3342; Lode et al. (1998) Cancer Res. 58:2925-2928). See alsoU.S. Pat. Nos. 5,714,586, 5,712,374, 5,264,586, and 5,773,001.

Enzymatically active toxins and fragments thereof which can be used aredescribed above and include diphtheria A chain, nonbinding activefragments of diphtheria toxin, exotoxin A chain (from Pseudomonasaeruginosa), ricin A chain, abrin A chain (from Corrybacteriumtyphimuriae), modeccin A chain, alpha-sarcin, Aleurites fordii proteins,dianthin proteins, Phytolaca americana proteins (PAPI, PAPII, andPAP-S), momordica charantia inhibitor, curcin, crotin, sapaonariaofficinalis inhibitor, gelonin, mitogellin, restrictocin, phenomycin,enomycin and the tricothecenes. See, for example, WO 93/21232 publishedOct. 28, 1993.

The present invention further contemplates a conjugate formed betweenactive compounds and an antibody or a compound with nucleolytic activity(e.g., a ribonuclease or a DNA endonuclease such as a deoxyribonuclease;DNase).

A variety of radioactive isotopes or radionuclides are available for theproduction of radioconjugated compounds as described above.

In some embodiments, conjugates of a targeting agent and therapeuticagents or detectable groups may be made using a variety of bi-functionalprotein coupling agents such asN-succinimidyl-3-(2-pyridyldithiol)propionate (SPDP),succinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate,iminothiolane (IT), bifunctional derivatives of imidoesters (such asdimethyl adipimidate HCL), active esters (such as disuccinimidylsuberate), aldehydes (such as glutareldehyde), bis-azido compounds (suchas bis(p-azidobenzoyl)hexanediamine), bis-diazonium derivatives (such asbis-(p-diazoniumbenzoyl)-ethylenediamine), diisocyanates (such astolyene 2,6-diisocyanate), and bis-active fluorine compounds (such as1,5-difluoro-2,4-dinitrobenzene). For example, a ricin conjugate can beprepared as described in Vitetta et al. (1987) Science 238:1098.Carbon-14-labeled 1-isothiocyanatobenzyl-3-methyldiethylenetriaminepentaacetic acid (MX-DTPA) is an exemplary chelating agent forconjugation of radionucleotide to the targeting peptide. See WO94/11026. The linker may be a “cleavable linker” facilitating release ofthe cytotoxic drug in the cell. For example, an acid-labile linker,peptidase-sensitive linker, dimethyl linker or disulfide-containinglinker (Chari et al. (1992) Cancer Res. 52:127-131) may be used.

Alternatively, a fusion protein including the targeting agent andtherapeutic agent or detectable group may be made, e.g. by recombinanttechniques or peptide synthesis.

In yet another embodiment, the targeting agent may be conjugated to a“receptor” (such as streptavidin) for utilization in tumor pre-targetingwherein the antibody-receptor conjugate is administered to the patient,followed by removal of unbound conjugate from the circulation using aclearing agent and then administration of a “ligand” (e.g., avidin)which is conjugated to a cytotoxic agent (e.g., a radionucleotide).

In some embodiments, the targeting peptide is fused to a Pseudomonasexotoxin or Diphtheria toxin. (U.S. Pat. No. 5,328,984 to Pastan et al.and U.S. Pat. No. 6,296,843 to Debinski). Pseudomonas exotoxins include,but are not limited to, Pseudomonas exotoxin A (PE). The Pseudomonasexotoxin can be modified such that it substantially lacks domain Ia, andPseudomonas exotoxins may further include PE38QQR and PE4E. Diphtheriatoxins include DT390, a diphtheria toxin in which the native bindingdomain is eliminated. It will be appreciated that the toxin can beconnected to either of the amino terminus, or the carboxyl terminus.

The present invention further contemplates a fusion protein comprising,consisting of, or consisting essentially of the targeting protein and acytosol localization element, which can be made by, for example,recombinant techniques or peptide synthesis. In some embodiments thisfusion protein also comprises, consists of, or consists essentially ofan effector molecule.

“Cytosol localization element” (also referred to as an endosomal exitelement) as used herein refers to an amino acid sequence used to directa target protein, fusion protein, or fragment thereof to the cytoplasm.The amino acid sequence can be of any size and composition, for example3 to 100 amino acids in length to, 4, 5, 6, 7, 8, 10, 12, 15, 20, 25,30, 40, 50, 60, 70, 80, 90 or 100 amino acids in length. In someembodiments the cytosol localization element enables the fusion proteinor a fragment thereof to exit an endocytic compartment after beinginternalized in the process of receptor-mediated internalization andenter the cytoplasm. In some embodiments the cytosol localizationelement is proteolytically activated, such as, but not limited to, by acalcium-dependent serine endoprotease, such as furin. Exemplary cytosollocalization elements include, but are not limited to cytosollocalization elements of bacterial toxins. Such bacterial toxinsinclude, but are not limited to Pseudomonas exotoxin A (PE), Diphtheriatoxin (DT), and Ricin A chain. Additional examples are described in: B.Beaumelle et al., Selective translocation of the A chain of Diphtheriatoxin across the membrane of purified endosomes. I Biol. Chem.267:11525-11531 (1992); I. Madshus et al., Membrane translocation ofDiphtheria toxin carrying passenger protein domain, Inf. Immun.60:3296-3302 (1992); H. Stenmark et al., Peptides fused to theamino-terminal end of Diphtheria toxin are translocated to the cytosol,J. Cell Biol. 113:1025-1032 (1991); and R. Chignola et al.,Self-potentiation of ligand-toxin conjugates containing Ricin A chainfused with viral structures, J Biol Chem 270:23345-23351 (1995). Stillother exemplary cytosol localization elements include those describe inU.S. Pat. No. 6,235,526, which is incorporated herein by reference.

The present invention further contemplates a fusion protein comprising,consisting of, or consisting essentially of the targeting protein and asubcellular compartment localization signal element, which can be madeby, for example, recombinant techniques or peptide synthesis. In someembodiments this fusion protein also comprises, consists of, or consistsessentially of a cytosol localization element and optionally an effectormolecule.

“Subcellular compartment localization signal element” as used hereinrefers to a signal sequence or tag used to direct a target protein,fusion protein, or fragment thereof to particular cellular organelles.In some embodiments the subcellular compartment localization signalelement comprises a peptide sequence. Such peptide sequences can be ofany size and composition, for example 3 to 100 amino acids in length to,4, 5, 6, 7, 8, 10, 12, 15, 20, 25, 30, 40, 50, 60, 70, 80, 90 or 100amino acids in length. Exemplary cellular organelles include, but arenot limited to, the nucleus, endoplasmic reticulum, golgi apparatus,endosomes, lysosomes, peroxisomes and mitochondria. Various subcellularcompartment localization signal elements are known and/or commerciallyavailable. Exemplary subcellular compartment localization signalelements include, but are not limited to, nuclear localization signalsand lysosomal localization signals. Other exemplary subcellularcompartment localization signal elements include those described in U.S.Pat. No. 7,585,636, which is incorporated herein by reference.

“Nuclear localization signals” as used herein refers to an amino acidsequence which directs a target protein, fusion protein, or fragmentthereof into the nucleus of a cell. Generally, nuclear localizationsignals (NLS) are a class of short amino acid sequences which may beexploited for cellular import of linked or coupled cargo into thenucleus. Such amino acid sequences can be from 3 to 100 amino acids inlength to 3 to 50, 4 to 30, or 4 to 20 amino acids in length. Thenuclear localization sequences of the present invention can be: (i) amonopartite nuclear localization sequence exemplified by the SV40 largeT antigen NLS (PKKKRKV) (SEQ ID NO: 55); (ii) a bipartite motifconsisting of two basic domains separated by a variable number of spaceramino acids and exemplified by the Xenopus nucleoplasmin NLS(KRXXXXXXXXXXKKKL) (SEQ ID NO: 56); or (iii) noncanonical sequences suchas M9 of the hnRNP A1 protein, the influenza virus nucleoprotein NLS,and the yeast Gal4 protein NLS (Dingwall and Laskey, Trends Biochem Sci16:478-481, 1991). In some embodiments, the nuclear localization signalis a highly cationic or basic peptide. In other embodiments the NLScomprises two or more Arg or Lys amino acid residues. In furtherembodiments of the present invention the NLS sequence binds to cytosolicproteins, such as importins and karyopherins, which recognize andtransport NLS-containing proteins or peptides to the nuclear porecomplex. The present invention envisions the use of any nuclearlocalization signal peptide, including but not limited to, SV40 virusT-antigen NLS and NLS sequences domain derived from viral Tat proteins,such as HIV Tat. Other exemplary nuclear localization signals include,but are not limited to those discussed in Cokol et al., 2000, EMBOReports, 1(5):411-415, Boulikas, T., 1993, Crit. Rev. Eukaryot. GeneExpr., 3:193-227, Collas, P. et al., 1996, Transgenic Research, 5:451-458, Collas and Alestrom, 1997, Biochem. Cell Biol. 75: 633-640,Collas and Alestrom, 1998, Transgenic Research, 7: 303-309, Collas andAlestrom, 1996, Mol. Reprod. Devel., 45:431-438, and U.S. Pat. Nos.7,531,624, 7,498,177, 7,332,586, and 7,550,650, all of which areincorporated by reference in their entireties.

“Lysosomal localization signal” as used herein refers to an amino acidsequence which directs a target protein or fusion protein to lysozymes.Examples include, but are not limited to, lysosome associated membraneprotein 1 (LAMP-1) tail sequence: RKRSHAGYQTI (SEQ ID NO: 57); lysosomalacid phosphatase (LAP): RLKRMQAQPPGYRHVADGEDHAV (SEQ ID NO: 58), andlysosomal integral membrane protein 2 (LIMP-2): RGQGSTDEGTADERAPLIRT(SEQ ID NO: 59).

In some embodiments of the present invention the fusion proteincomprises, consists of, or consists essentially of a targeting protein,a cytosol localization element, a subcellular compartment localizationsignal element, and optionally an effector molecule. These componentsmay be coupled to one another in any order that allows for the targetingprotein to bind to its receptor and further allows for the transport ofthe fusion protein or a fragment thereof into the nucleus.

In further embodiments of the present invention the fusion proteincomprises, consists of, or consists essentially of a targeting proteincomprising IL-13, a mutant of IL-13 or an analogue or fragment thereof;a cytosol localization element comprising Pseudomonas exotoxin A (PE) orDiphtheria toxin (DT); and a subcellular compartment localization signalelement comprising a nuclear localization signal or a lysosomallocalization signal. In other embodiments of the present invention thefusion protein comprises, consists of, or consists essentially ofIL-13.E13K, the cytosol bacterial toxin domain D2 of PE, and a nuclearlocalization signal from the SV40 T antigen. In one embodiment of thepresent invention the fusion protein is a single-chain recombinantprotein comprising, consisting of, or consisting essentially of, fromthe N-terminus to the C-terminus, IL-13.E13K, the cytosol bacterialtoxin domain D2 of PE, and a nuclear localization signal from the SV40 Tantigen, i.e. IL-13.E13K-D2-NLS.

E. PHARMACEUTICAL FORMULATIONS AND METHODS

The active compounds, conjugates, and/or compositions thereof describedherein may be formulated for administration in a pharmaceutical carrierin accordance with known techniques. See, e.g., Remington, The Scienceand Practice of Pharmacy (9^(th) Ed. 1995). In the manufacture of apharmaceutical formulation according to the invention, the activecompound(s) (including the physiologically acceptable salts thereof) istypically admixed with, inter alia, an acceptable carrier. The carriermust, of course, be acceptable in the sense of being compatible with anyother ingredients in the formulation and must not be deleterious to thepatient. The carrier may be a solid or a liquid, or both, and ispreferably formulated with the compound(s) as a unit-dose formulation,for example, a tablet, which may contain from 0.01 or 0.5% to 95% or 99%by weight of the active compound. One or more active compounds may beincorporated in the formulations of the invention, which may be preparedby any of the well-known techniques of pharmacy comprising admixing thecomponents, optionally including one or more accessory ingredients.

The formulations of the invention include those suitable for oral,rectal, topical, buccal (e.g., sub-lingual), vaginal, parenteral (e.g.,subcutaneous, intramuscular, intradermal, or intravenous), topical(i.e., both skin and mucosal surfaces, including airway surfaces) andtransdermal administration, although the most suitable route in anygiven case will depend on the nature and severity of the condition beingtreated and on the nature of the particular active compound which isbeing used.

Particular routes of parenteral administration include intrathecalinjection, including directly into the tumor or a tumor resectioncavity, and intraventricular injection into a ventricle of the brain.

Active compounds and compositions may be administered by intratumorinjection (including tumors in any region such as tumors of the brain),or in the case of brain tumors injection into a ventricle of the brain.

Formulations of the present invention suitable for parenteraladministration comprise sterile aqueous and non-aqueous injectionsolutions of the active compound, which preparations are preferablyisotonic with the blood of the intended recipient. These preparationsmay contain anti-oxidants, buffers, bacteriostats and solutes thatrender the formulation isotonic with the blood of the intendedrecipient. Aqueous and non-aqueous sterile suspensions may includesuspending agents and thickening agents. The formulations may bepresented in unit\dose or multi-dose containers, for example sealedampoules and vials, and may be stored in a freeze-dried (lyophilized)condition requiring only the addition of the sterile liquid carrier, forexample, saline or water-for-injection immediately prior to use.Extemporaneous injection solutions and suspensions may be prepared fromsterile powders, granules and tablets of the kind previously described.For example, in one aspect of the present invention, there is providedan injectable, stable, sterile composition comprising an active compoundor composition in a unit dosage form in a sealed container. The compoundor composition is provided in the form of a lyophilizate that is capableof being reconstituted with a suitable pharmaceutically acceptablecarrier to form a liquid composition suitable for injection thereof intoa subject. The unit dosage form typically comprises from about 10 mg toabout 10 grams of the compound or composition. When the compound orcomposition is substantially water-insoluble, a sufficient amount ofemulsifying agent that is physiologically acceptable may be employed insufficient quantity to emulsify the compound or composition in anaqueous carrier. One such useful emulsifying agent is phosphatidylcholine.

Further, the present invention provides liposomal formulations of thecompounds disclosed herein and compositions thereof. The technology forforming liposomal suspensions is well known in the art. When thecompound or composition thereof is an aqueous-soluble composition, usingconventional liposome technology, the same may be incorporated intolipid vesicles. In such an instance, due to the water solubility of thecompound or composition, the compound or composition will besubstantially entrained within the hydrophilic center or core of theliposomes. The lipid layer employed may be of any conventionalcomposition and may either contain cholesterol or may becholesterol-free. When the compound or composition of interest iswater-insoluble, again employing conventional liposome formationtechnology, the composition may be substantially entrained within thehydrophobic lipid bilayer that forms the structure of the liposome. Ineither instance, the liposomes that are produced may be reduced in size,as through the use of standard sonication and homogenization techniques.

Liposomal formulations containing the compounds disclosed herein orcompositions thereof (e.g., IL-13 conjugates, such asIL-13.E13K-D2-NLS), may be lyophilized to produce a lyophilizate, whichmay be reconstituted with a pharmaceutically acceptable carrier, such aswater, to regenerate a liposomal suspension. Examples of liposomalformulations that can be used include the neutral lipid1,2-dioleoyl-sn-glycero-3-phosphatidylcholine (DPOC) (See, e.g., LandenJr. et al. (2005) Cancer Res. 65:6910-6918).

Other pharmaceutical compositions may be prepared from thewater-insoluble compounds disclosed herein, or compositions thereof,such as aqueous base emulsions. In such an instance, the compositionwill contain a sufficient amount of pharmaceutically acceptableemulsifying agent to emulsify the desired amount of the compound orcomposition thereof. Particularly useful emulsifying agents includephosphatidyl cholines, and lecithin.

In addition to active compounds, the pharmaceutical compositions maycontain other additives, such as pH-adjusting additives. In particular,useful pH-adjusting agents include acids, such as hydrochloric acid,bases or buffers, such as sodium lactate, sodium acetate, sodiumphosphate, sodium citrate, sodium borate, or sodium gluconate. Further,the compositions may contain microbial preservatives. Useful microbialpreservatives include methylparaben, propylparaben, and benzyl alcohol.The microbial preservative is typically employed when the formulation isplaced in a vial designed for multidose use. Of course, as indicated,the pharmaceutical compositions of the present invention may belyophilized using techniques well-known in the art.

The therapeutically effective dosage of any one active agent, the use ofwhich is in the scope of present invention, will vary somewhat fromcompound to compound, and patient to patient, and will depend uponfactors such as the age and condition of the patient and the route ofdelivery. Such dosages can be determined in accordance with routinepharmacological procedures known to those skilled in the art.

As a general proposition, the initial pharmaceutically effective amountof the active compound or composition administered parenterally will bein the range of about 0.1 to 50 mg/kg of patient body weight per day,with the typical initial range of antibody used being 0.3 to 20mg/kg/day, more preferably 0.3 to 15 mg/kg/day. The desired dosage canbe delivered by a single bolus administration, by multiple bolusadministrations, or by continuous infusion administration of activecompound, depending on the pattern of pharmacokinetic decay that thepractitioner wishes to achieve.

The active compound(s) is suitably administered to the patient at onetime or over a series of treatments. Depending on the type and severityof the disease, about 1 μg/kg to 15 mg/kg (e.g. 0.1-20 mg/kg) of activecompound(s) is an initial candidate dosage for administration to thepatient, whether, for example, by one or more separate administrations,or by continuous infusion. A typical daily dosage might range from about0.1, 0.5, 1, 10 or 100 μg/kg up to 100, 200 or 500 mg/kg, or more,depending on the factors mentioned above. For repeated administrationsover several days or longer, depending on the condition, the treatmentis sustained until a desired suppression of disease symptoms occurs. Amore particular dosage of the active compound will be in the range fromabout 0.05 mg/kg to about 10 mg/kg. Thus, one or more doses of about 0.5mg/kg, 2.0 mg/kg, 4.0 mg/kg or 10 mg/kg (or any combination thereof) maybe administered to the patient. Such doses may be administeredintermittently, e.g. every week or every three weeks (e.g., such thatthe patient receives from about two to about twenty, e.g. about sixdoses of the anti-ErbB2 antibody). An initial higher loading dose,followed by one or more lower doses may be administered. An exemplarydosing regimen comprises administering an initial loading dose of about0.5 to 10 mg/kg, followed by a weekly maintenance dose of about 0.5 to10 mg/kg of the active compound. However, other dosage regimens may beuseful. The progress of this therapy is easily monitored by conventionaltechniques and assays.

Subjects treated by the methods of the present invention can also beadministered one or more additional therapeutic agents. See U.S. Pat.No. 5,677,178. Chemotherapeutic agents may be administered by methodswell known to the skilled practitioner, including systemically, directinjection into the cancer, or by localization at the site of the cancerby associating the desired chemotherapeutic agent with an appropriateslow release material or intra-arterial perfusing of the tumor. Thepreferred dose may be chosen by the practitioner based on the nature ofthe cancer to be treated, and other factors routinely considered inadministering. See, e.g., U.S. Pat. No. 7,078,030.

Subjects may also be treated by radiation therapy, including, but notlimited to, external beam radiotherapy, which may be at any suitabledose (e.g., 20 to 70 Gy or more per tumor, typically delivered over afractionated schedule).

Pharmaceutical compositions containing targeting agent in unlabeled formmay be administered to subjects as blocking reagents, in like manner asdescribed in Abrams et al., U.S. Pat. No. RE38,008, in conjunction withthe administration of targeting agent coupled to a therapeutic group.

Targeting peptide coupled to a diagnostic group may also be used invitro as histological reagents on tissue samples, where binding of theIL-13 receptor is indicative of cancer tissue in the tissue sample.

Examples Materials and Methods

Cell Culture.

Human GBM cell lines U-251 MG and LN229 were obtained from American TypeCulture Collection (Manassas, Va.). U-251 MG cells were maintained inDMEM (Lonza, Walkersville, Md.) supplemented with 1× non-essential aminoacid (Invitrogen, Carlsbad, Calif.) and 10% FCS (Hyclone, Logan, Utah).LN229 cells were grown in DMEM supplemented with 10% FCS. G48a cellswere grown and maintained in RPMI 1640 (Lonza, Walkersville, Md.)supplemented with glucose, adjusted to 4 gm/litre of media and 10% FCS(13).

Cloning, Production and Purification of Targeted Proteins.

A duplex primer cloning strategy was employed wherein SV40 T-antigen NLS5′ and 3′ sequence primers were synthesised (Invitrogen) and made intoduplex DNA (containing Xho1/BamH1 ends) by incubating the primers infavorable annealing conditions. The annealed duplex was then subclonedinto the IL-13-D2 containing plasmid using Xho1/BamH1 at the 3′ end toproduce IL-13-D2-NLS. The IL-13-D2 plasmid was engineered by sub-cloningit from a previously generated IL-13-D2-PE38QQR plasmid (24). The IL-13mutant recombinant constructs were made by replacing the wild type IL-13sequence from the parent plasmid with the mutant IL-13 sequence (25).The NH2-terminal end of NLS domain was joined to the COOH terminal ofIL-13.E13K domain using the HindIII site to form the IL-13.E13K-NLSplasmid. Also, all of these recombinant constructs were transformed inDH5α E. coli cells for amplification. All the constructs were sequencedat DNA sequencing Laboratory of the Comprehensive Center of Wake ForestUniversity and analyzed for their in-frame DNA sequence using anautomated sequence analyzer prior to protein expression.

Also, the IL-13/IL-13.E13K-D2-NLS and other control DNA constructs havebeen created in a manner such that it enables the expression of theseproteins under the IPTG inducible T7 promoter in BL21 (λDE3) E. coliprotein expression system as previously described (33). In brief, therecombinant constructs were transformed in BL21 cells and the cells weregrown in Luria-broth media supplemented with 100 μg/ml of ampicillin at37° C. shaker. When the A600 of the bacterial culture media reachedaround 1.4, the recombinant protein expression in the cells was inducedby addition of 1 nmol/L of IPTG and allowed to incubate for further 90min. The expressed proteins in the inclusion bodies were then denaturedusing 7 M Guanidine (MP Biomedicals, Salon, Ohio) and1,4-Dithiothr.eitol (Sigma, St. Louis, Mo.). The reduced protein wasthen renatured in a buffer containing arginine/L-glutathione oxidase(Sigma, St. Louis, Mo.). The protein was further dialyzed and purifiedby SP Sepharose ion-exchange liquid chromatography (GE Healthcare,Piscataway, N.J.) using Fast Protein Liquid Chromatography system (GEHealthcare, Piscataway, N.J.). The purified proteins were subsequentlyrun on SDS-PAGE gels to identify the purity of the isolated proteins.All the proteins obtained were >90% pure.

Colorimetric MTS/PMS Cell Viability Assay.

1×103 U-251 MG cells were plated per well in quadruplicates for eachconcentration to be tested. IL-13.E13K-PE38QQR is an IL-13Rα2 basedcytotoxin against GBM (24). After 24 hours incubation at 37° C. for thecells to attach, a fixed concentration (i.e. 1 μM) of theIL13.E13K-D2-NLS and other purified proteins were added and incubated at37° C. for 1 hr. After 1 hr. incubation, increasing concentrations ofthe IL-13.E13K-PE38QQR ranging from 0.1 to 100 ng/ml was added and theplate was incubated for 48 hr. Cells treated with cyclohexamide and justthe cytotoxins were used as controls. After 48 hr., cell viability wasmeasured using the MTS[3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium]PMS [phenazine methosulfate] dye (Promega, Madison, Wis.) as per themanufacturer's instructions. The absorbance from the assay was measuredat 490 nm using the plate reader Spectra max 340 PC (Molecular Devices,Sunnyvale, Calif.) and data was plotted as percentage of control versusconcentration of the toxin used.

IL-13-D2-NLS and IL-13-D2 Labeling with EDC-Sulpho-NHS and Alexa Fluor488 Labels.

Purified IL-13-D2-NLS and the IL-13-D2 proteins were labeled at theircarboxylate amino acids via EDC(1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride). EDCreacts with a carboxyl group on an amino acid of the protein and formsan amine reactive O-acylisourea intermediate that swiftly reacts with anamino group to form an amide bond and release the isourea by-product.The intermediate is unstable in aqueous solutions and therefore,two-step conjugation procedures require N-hydroxysuccinimidestabilization (Sulfo-NHS). Sulfo-NHS reacts with the O-acylisoureaintermediate and stabilizes it. Next, Alexa fluor 488-hydrazide wasadded, which replaced the Sulfo-NHS and formed a stable amide bond onthe carboxyl groups of the protein to form labeled protein conjugates.

The proteins were initially dissolved in the activation buffer (0.05 MMES, 0.5 M NaCl, pH 6) at the concentration of 1 mg/ml usingbuffer-exchange columns. Later 2 mM EDC and 5 mM Sulfo-NHS (ThermoScientific, Waltham, Mass.) were added to the proteins and allowed toreact for 15 min at RT. Subsequently, 0.14 μl of 2-mercaptoethanol wasadded to quench the unreacted EDC. The protein-EDC-Sulfo-NHS conjugateswere then dissolved in the coupling buffer (0.1 M sodium phosphate, 0.15M NaCl, pH 7.5) using buffer exchange columns (Pierce, Rockford, Ill.).Next, alexa fluor 488 hydrazide (dissolved in the coupling buffer)(Invitrogen, Carlsbad, Calif.) was added at 25 molar concentrationexcess to the proteins and incubated in the dark at RT for 30 minutes.After incubation, 10 mM hydroxylamine (Thermo Scientific, Rockford,Ill.) was added to quench the excess fluor. The excess unreactedhydrazide fluor was removed using Pierce protein desalting columns.

Localization Studies of the Labeled Proteins on IL-13Rα2 Positive U-251MG Cells Using Alexa Fluor 488 EDC-Sulfo-NHS Labeled Proteins.

25,000 U-251 MG GBM cells were plated on coverslip/per well in a 24-wellplate. The cells were allowed to adhere to the coverslips for 24 hr.,after which 500 nM each of the EDC-Sulpho-NHS labeled proteins wereadded to the U-251 MG cells for 15 min and 4 hr. After the incubations,the cells were fixed with acetone (pre-chilled at −20° F.) for 10 minsand washed with PBS 4× times. The coverslips were then mounted on theslides using the gel mount (Biomeda, Foster City, Calif.) and observedwith LSM 510 Zeiss Confocal Microscope (Cellular Imaging Core,Comprehensive Cancer Center, Wake Forest University) and the imagesprocessed using Zeiss LSM Image Browser (version 4.2).

Direct Labeling of IL-13.E13K-D2-NLS and IL-13.E13K-D2 with Alexa FluorLabels.

The proteins were directly labeled with alexa fluor 488 dye using theAlexa fluor 488 microscale protein labeling kit from Invitrogen(Carlsbad, Calif.) as per the manufacturer's instructions. A molar ratioof 25 of the dye to the protein was used to label both the proteins. Theproteins were run on 12% SDS-PAGE gel. The gel was scanned using Typhoon9210 (Amersham Pharmacia Biotech) for fluorescence signals and laterstained using coomassie blue dye.

Localization Studies of the Labeled Proteins on IL-13Rα2 Positive U-251MG Cells for Alexa Fluor 488 Directly Labeled Proteins.

25,000 U-251 MG GBM cells were plated on coverslips per well in a24-well plate. After 24 hr. for allowing the cells to adhere and attachto the plate, 1 μM/well of alexa fluor directly labeled proteins wereadded to the U-251 MG cells for 15 min and 4 hr. After the incubations,the cells were fixed with 5% paraformaldehyde (Ted Pella, Redding,Calif.) for 15 mins at 37° C. and washed with 1×PBS (3 times). The cellswere then permeabilized with 0.1% Triton-X-100/0.2% BSA-PBS for 10 mM atRT. After permeabilization, the cells were washed 3 times with 1×PBS.Subsequently, Topro-3 iodide (Invitrogen, Carlsbad, Calif.) was added ata concentration of 1:1000 dilution of the 1 mM stock to stain the cellnuclei. The coverslips were then mounted on the slides using the gelmount (Biomeda, Foster City, Calif.) and observed with LSM 510 ZeissConfocal Microscope (Cellular Imaging Core, Comprehensive Cancer Center,Wake Forest University) and the images processed using Zeiss LSM ImageBrowser (version 4.2).

Direct Labeling of IL-13.E13K-D2-NLS and IL-13.E13K-D2 with Biotin andTyramide Signal Amplification System.

Biotin-XX microscale protein labeling kit (Invitrogen, Carlsbad, Calif.)was used to label the proteins as per the manufacturer's instructions. Adifferent molar ratio of 12, 8 or 4 biotin-dye to the proteins was used.The biotin-labeled proteins were run on a gel and a western blot carriedout using streptavidin-HR.P (Pierce, Rockford, Ill.) to detect forbiotin-labeled proteins. The number of Biotin molecules attached to theproteins was determined by the Biofluoreporter assay kit (Invitrogen) asper the manufacturer's guidelines.

Localization Studies of the Labeled Proteins on IL-13Rα2 Positive U-251MG Cells for Biotin-Conjugated Proteins.

12,500 U-251 MG GBM cells were plated on coverslips per well in a24-well plate. After 24 hr., 1 μM/well of biotin-labeled proteins wasadded onto the U-251 MG cells for 15 min, 4, 8 and 24 hr. After theincubations, the cells were fixed with 4% paraformaldehyde (Ted Pella,Redding, Calif.) for 15 mins at 37° C. and washed with PBS 4× times. Thecells were then permeabilized with 0.1% Triton-X-100/0.2% BSA-PBS for 10min at RT. After permeabilization, the cells were washed 3 times with1×PBS. After washings, Tyramide signal amplification kit (Invitrogen,Carlsbad, Calif.) using Alexa fluor 488 dyes and HR.P-streptavidin wascarried out as per manufacturer's instructions. Topro-3 iodide(Invitrogen, Carlsbad, Calif.) was added at a concentration of 1:1000dilution of the 1 mM stock to stain the cell nuclei. After the tyramidestaining, wells were washed and mounted with gel mount (Biomeda, FosterCity, Calif.) and observed with LSM 510 Zeiss Confocal Microscope(Cellular Imaging Core, Comprehensive Cancer Center, Wake ForestUniversity) and the images processed using Zeiss LSM Image Browser(version 4.2).

Immunoblotting.

500 ng/well of each of the recombinant biotin conjugated proteins wereloaded onto a 12% SDS-PAGE gel and transferred to a polyvinylidenedifluoride membrane (Perkin Elmer, Shelton, Conn.). Blots were blockedwith 5% milk-phosphate buffered saline (PBS) for 1 hr. at roomtemperature (RT). Biotin-proteins were detected using streptavidinconjugated with horseradish peroxidase (Thermo Fisher Scientific,Rockford, Ill.) diluted 1:16000 in blocking buffer. The detection wasperformed using an ECL plus kit (GE Healthcare).

Results

Production of IL-13.E13K-D2-NLS, IL-13.E13K-D2, IL-13.E13K-NLS andIL-13.E13K Proteins.

We aim at developing effective drug/radioactive isotope deliveryvehicles to specific intracellular compartments of a cancer cell, basedpreferentially on recombinant proteins. Hence, we have developed here arecombinant protein delivery vehicle to the nuclei of GBM cells. Thisdelivery vehicle recognizes the IL-13Rα2, which is overexpressed on GBMcells. The IL-13.E13K-D2-NLS recombinant protein recognizes IL-13Rα2 andis internalized into the GBM cells, exits endosomes and is trafficked tothe cell's nuclei. IL-13.E13K-D2-NLS and its control proteins,IL-13.E13K-NLS and IL-13.E13K-D2 as well as IL-13.E13K, which are notexpected to either leave the endosomal compartment or reach the nucleus,respectively were produced in E. coli and purified using the FPLCsystem. IL-13.E13K-D2-NLS was highly inducible in BL21 E. coli cells.The induced protein was isolated and further processed using adisulphide-shuffling method and purified using FPLC column, as describedpreviously (25; 34). Even with the first step of purification, theprotein was highly purified. The control IL-13.E13K-D2, theIL-13.E13K-NLS and the IL-13.E13K recombinant proteins were expressed,processed and purified in a similar manner.

IL-13.E13K-D2-NLS, IL-13.E13K-D2, IL-13.E13K-NLS and IL-13.E13K Competefor IL-13Rα2 on GBM Cells.

We next wished to confirm that all the purified recombinant proteinsbind to the IL-13Rα2 receptor on GBM cells. To this end, we carried outa cell-viability assay in which these recombinant proteins bound to theIL-13Rα2 receptor and protected against cytotoxic action ofIL-13.E13K-PE38QQR. IL-13.E13K-PE38QQR, as mentioned earlier, is arecombinant cytotoxin that binds to the IL-13Rα2, is internalized intocells leading to cell killing through the cleaved active portion of PE,enzymatic domain III. As expected, all recombinant proteins of interestblocked the action of the cytotoxin, resulting in no cell killing:IL13.E13K-D2-NLS; IL-13.E13K-D2; IL-13.E13K-NLS and IL-13.E13K. Theseresults confirm that all the recombinant proteins retain IL-13.E13Kligand binding properties and compete specifically for the IL-13Rα2.

IL-13.E13K-D2-NLS Localizes to the Nuclei of U-251 MG GBM Cells.

Next, we wished to monitor the intracellular journey as well as thesubcellular localization of our targeted proteins. To this end, wefluorescently labeled these proteins using three differentapproaches/methods. For the first approach, we labeled the carboxylamino acids of the proteins, so as not to modify the primary amines(lysines) present in the NLS domain of the protein. Thus, we utilizedthe Sulfo-NHS-EDC and Alexa fluor 488 labeling techniques. IL-13-D2-NLSand IL-13-D2 were labeled at their carboxylate groups on amino acidswith alexa fluor 488 via EDC(1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride andSulfo-NHS (N-hydroxysuccinimide) (see Materials and Methods). In thesecond approach, we directly labeled the primary amines of the proteins,which are present also in the lysines, with the Alexa Fluor 488-TFPreactive dyes. And for the third approach, we carried out an indirectlabeling method; here we initially conjugated our proteins at theprimary amines with biotin molecules to make biotinylated-proteins.These biotinylated-proteins were then used for cell localizationexperiments, later the biotin molecules were detected usingHRP-Streptavidin and the signal amplified using Tyramide signalamplification method.

After labeling the proteins using the first conjugation method, i.e.EDC-Sulfo-NHS Alexa fluor 488 labeling, we performed cell localizationexperiments in U-251 MG GBM cells. We observed that the IL-13-D2-NLSeffectively localized to the nucleus at 1 hr., preceded by membrane andcytosolic localization at 15 min. We also performed Z-stack analysis toconfirm the localization of the protein inside the nucleus. The Z-stackanalysis demonstrated a nuclear localization of IL-13.E13K-D2-NLS (datanot shown). On the other hand, IL-13-D2 did get internalized into theU-251 MG cells and was found to be in the cytosol, primarily in theperi-nuclear region, but it did not travel into the nucleus at either 15min or 1 hr. of the experiment.

The above experiments strongly suggested an ability of IL-13-D2-NLS, butnot IL-13-D2, to localize to U-251 GBM cells' nuclei. However, in orderto obtain higher resolution pictures, we carried out a direct labelingof IL-13.E13K-D2-NLS and IL-13.E13K-D2 with the Alexa-fluor 488 dye. Inthis second approach, Alexa fluor 488 tetrafluorophenyl (TFP) reactivedye molecules attach directly to the primary amines of the amino acidsof the proteins forming stable protein-dye conjugates. The protein-dyeconjugates were visualized using either Coomassie-stained SDS-PAGE orfluorescence signals using Typhoon imaging system. The Typhoon scanshowed protein-dye conjugates emitting fluorescence signals, while theunconjugated proteins did not produce any signals (not shown). We nextrepeated the localization experiments in U-251 MG cells and found whatwe had observed earlier. IL-13.E13K-D2-NLS localized to the nuclei at 1hr. (not shown) whereas IL-13.E13K-D2 protein never trafficked into thenucleus.

In order to examine whether yet another visualization method woulddocument the same nuclei-localization ability of our recombinantconstructs; we decided to use a signal amplification method via tyramidemolecules. We initially labeled our proteins using biotin-XXsulfosuccinimidyl ester (biotin-XX, SSE); which reacts very efficientlywith the primary amines of the proteins forming stable protein-biotinconjugates. The biotinylated proteins were analyzed usingSDS-PAGE/Western blot and the protein-biotin conjugates were detectedusing streptavidin-HRP. The Western blot indicated that both theproteins had been biotinylated. The number of biotins on each of theseproteins was quantified by performing FluoReporter Biotin Quantitationassay based on standard curve. Using a quadratic fit equation, theIL-13.E13K-D2-NLS and IL-13.E13K-D2 had a similar degree of labeling(DOL) of 13.87 and 14.45 when labeled at a protein to dye molar ratio of1:4 and 1:8, respectively. Next, these biotinylated proteins were testedin a neutralization of cytotoxicity assay (not shown). BothIL-13.E13K-D2-NLS and IL-13.E13K-D2 biotinylated proteins blocked theaction of IL-13Rα2-specific cytotoxin-mediated U-251 MG cell killingindicating that these conjugates still compete for the receptor afterundergoing biotinylation. The cell localization experiment was thenconducted and the proteins were detected using Alexa fluor 488 andHRP-Streptavidin tyramide signal amplification procedure (see theMethods section). We found that in the case of IL-13.E13K-D2-NLS, at 5min., the protein was bound to the cell membrane with some cytosoliclocalization. At 4 hr., cells had nuclear localization, whereas almostall the cells had a significant portion of the protein inside theirnuclei at 8 hr. and 24 hr. For the IL-13.E13K-D2, at 5 min the proteinwas mostly found bound to the cell membrane with some moleculesundergoing internalization. Whereas, at 8 and 24 hr. the protein waspredominantly internalized and localized in the perinuclear region ofcells. At 4 hr., the IL-13.E13K-D2 protein had cytosolic localization.Z-stack analyses of a 24 hr. experiment (not shown) establishes that theIL-13.E13K-D2 protein does not migrate to the nucleus.

We have also carried out experiments wherein we have labeled theseproteins with different molar ratios of the biotin-dye. The protein:dyeratios used were 12, 8 and 4. When both IL13.E13K-D2-NLS andIL-13.E13K-D2 proteins were labeled at dye molar ratio of 12, weobserved similar localization for these proteins as described, except wedid not observe any nuclear localization at 4 hours. When we went downon the amount of dye (protein:dye molar ratio of 8 and 4 respectively)we observed more cells having nuclear localization at 4 hr. (Data notshown).

We also carried out cell localization experiment with another controlprotein, IL-13.E13K-NLS, which is devoid of Domain 2 of PE and shouldnot be able to undergo endosomal translocation and subsequent nucleartransport; it should behave like the IL-13.E13K ligand alone. 12% SDSPAGE/Western blot of the IL-13.E1K-D2-NLS, IL-13.E13K-D2, IL-13.E13K-NLSand the IL-13.E13K proteins conjugated with biotin and probed withstreptavidin-HRP indicate that all the proteins are similarly labeledwith biotin and also all the biotin-conjugated proteins bind to theIL-13Rα2 on GBM cells. The studies with IL-13.E13K-NLS and IL-13.E13Kindicated our hypothesis to be correct, since this control protein diddemonstrate perinuclear localization, but no nuclear transport at 24 hr.The same was observed in the cell localization studies using just theIL-13.E13K ligand. The IL-13.E13K accumulated mainly in the peri-nuclearregion. Very few cells had these proteins in the nucleus. We have alsocarried out the localization studies for the IL-13.E13K-NLS andIL-13.E13K at 8, 4 hr and 5 min and they all demonstrate the resultsobserved at 24 hr. (Data not shown).

IL-13.E13K-D2-NLS Localizes to the Nucleus of G48a GBM Cells.

We repeated the above experiments in another GBM cell line, G48a (13),which over-expresses IL-13Rα2. We obtained similar results as with theU-251 MG cells. Again, almost all the cells had the IL-13.E13K-D2-NLSprotein inside their nuclei not only at 8 hr. and 24 hr., but already at4 hr. of the experiment. Again, at 5 min, we observed mainly plasmamembrane binding with some internalization of the protein. Z-stackanalysis for the 24 hr. experiment establishes nuclear localization ofthe IL-13.E13K-D2-NLS protein. Similar results were observed for theIL-13.E13K-D2, IL-13.E13K-NLS and IL-13.E13K proteins in G48 cells as inU-251 MG cells; IL-13.E13K-D2, as well as IL-13.E13K-NLS and IL-13.E13Kwere not found to have any nuclear localization at any of thetime-points and mainly had cytosolic/perinuclear localization with thetime of experiment at 4, 8 and 24 hr. and cell membrane binding at 5min.

IL-13.E13K-D2 NLS does not Localizes to the Nucleus of LN229 Cells.

We carried out identical experiments with biotin-labeledIL-13.E13K-D2-NLS in LN229 cells, very low expressors of IL-13Rα2. Weobserved that the protein displayed some binding to the cell surfacewith moderate internalization, but we did not observe any nuclearlocalization for the IL-13.E13K-D2-NLS protein at any of theexperimental time points and no cytosolic or perinuclear localizationfor the IL-13.E13K-D2, IL-13.E13K-NLS and IL-13.E13K at 24 hr. contraryto what we observed in IL-13Rα2 high expressors, U-251 MG and G48acells. Z-stack analysis for the IL-13.E13K-D2-NLS protein localizationin an LN229 cell at 24 hr. depicts low internalization and no nuclearlocalization for the protein in these cells.

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The foregoing is illustrative of the present invention, and is not to beconstrued as limiting thereof. The invention is defined by the followingclaims, with equivalents of the claims to be included therein.

That which is claimed is:
 1. A compound comprising, in combination: anIL-13Rα2 binding ligand; at least one effector molecule; a cytosollocalization element covalently coupled between said binding ligand andsaid at least one effector molecule; and a subcellular compartmentlocalization signal element covalently coupled between said bindingligand and said at least one effector molecule.
 2. A compound of claim1, wherein said compound has the formula, from N terminus to C terminus,selected from the group consisting of: A-B-C-D-E, E-D-C-B-A, A-B-D-C-E;and E-C-D-B-A, wherein: A is an IL-13Rα2 binding ligand; B is saidcytosol localization element; C is said subcellular compartmentlocalization signal element; D is present or absent and when present afirst effector molecule; and E is present or absent and when present isa second effector molecule.
 3. The compound of claim 1, wherein saidcompound is a fusion protein or covalent conjugate.
 4. The compound ofclaim 1, wherein each of A, B, and C, and optionally D and E, is aprotein or peptide.
 5. The compound of claim 1, wherein said cytosollocalization element is a Pseudomonas exotoxin or diphtheria toxintranslocation domain.
 6. The compound of claim 5, wherein said cytosollocalization element is a Pseudomonas exotoxin A D2 segment.
 7. Thecompound of claim 1, wherein said subcellular compartment localizationsignal element is a nuclear localization element or a lysosomallocalization element.
 8. The compound of claim 7, wherein saidsubcellular compartment localization signal element is an SV40 T antigennuclear localization signal.
 9. The compound of claim 1, wherein saidIL-13Rα2 binding ligand is IL-13, a mutant of IL-13, or an IL-13Rα2binding fragment thereof.
 10. The compound of claim 1, wherein said atleast one effector molecule consists of two effector molecules.
 11. Thecompound of claim 1, wherein D is a toxin and E when present is anamphipathic antimicrobial peptide.
 12. The compound of claim 11, whereinsaid toxin is selected from the group consisting of diphtheria toxin andPseudomonas exotoxin.
 13. The compound of claim 11, wherein saidamphipathic antimicrobial peptide comprises a sequence selected from thegroup consisting of: (KLAKLAK)₂ (SEQ ID NO: 60); (KLAKKLA)₂ (SEQ ID NO:61); (KAAKKAA)₂ (SEQ ID NO: 62) and (KLGKKLG)₂ (SEQ ID NO: 63).
 14. Thecompound of claim 1, wherein said at least one effector moleculecomprises a therapeutic agent, a detectable group, a lipid, or aliposome.
 15. A nucleic acid that encodes a compound of claim 1, andwherein said compound is a protein or peptide.
 16. A host cell thatcontains a nucleic acid of claim 15 and expresses the encoded peptide.17. A method of treating cancer in a subject in need thereof, comprisingadministering said subject a peptide of claim 1 in a treatment effectiveamount.
 18. The method of claim 17, wherein said cancer is selected fromthe group consisting of breast cancer, bladder cancer, pancreaticcancer, colorectal cancer, head and neck cancer, thyroid cancer,prostate cancer, and gliomas.
 19. The method of claim 18, wherein saidcancer is glioblastoma multiforme.
 20. A method of detecting IL-13Rα2expressing cells, comprising administering a compound of claim 1 to acell or group of cells and detecting a detectable group coupled to saidcompound.
 21. A method of delivering at least one effector molecule to asubcellular compartment of a cell of interest, comprising: contacting acompound of claim 1 including at least one effector molecule to a cellof interest under conditions in which said compound is internalizedtherein and said effector molecule is delivered to said subcellularcompartment.
 22. The method of claim 21, wherein said subcellularcompartment is the nucleus.
 23. The method of claim 22, wherein said atleast one effector molecule comprises a detectable group.
 24. The methodof claim 21, wherein said compound further comprises an additionaleffector molecule (e.g., as either D or E).
 25. The method of claim 24,wherein said additional effector molecules is delivered to the cytosolof said cell of interest (e.g., wherein said compound is of the formulaA-B-D-C-E or E-C-D-B-A).